ClinVar Miner

Submissions for variant NM_017636.4(TRPM4):c.1150+1G>A (rs200132598)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000625948 SCV000746543 likely pathogenic Progressive familial heart block type 1B 2017-12-03 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000728368 SCV000855928 uncertain significance not provided 2017-08-01 criteria provided, single submitter clinical testing

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